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α-GalCer analog 8 is a high purity, custom synthesis, synthetic α-galactocerebrosidase enzyme that has been modified to include 8 fluorine atoms. The enzyme is glycosylated at the N-terminal and methylated at the C-terminal. The modification of this enzyme with an oligosaccharide and monosaccharide moiety improves its stability in vivo. α-GalCer analog 8 is used for the treatment of Gaucher's disease, which is caused by the accumulation of complex carbohydrates in the body. This condition can be managed using α-GalCer analog 8 because it hydrolyzes these complex carbohydrates into their monosaccharides.

a-D-Mannose-1-phosphate bis(cyclohexylammonium) salt is a sugar that has the CAS number 51306-17-3 and is listed as a synthetic compound. It is a white to off-white powder that can be used in many different applications, including as an enzyme inhibitor, protein modifier, and prodrug. The modification of this sugar can include fluorination, glycosylation, methylation, or modification with other sugars. This product also has a high purity and custom synthesis.

Sialyl-dimeric Lex-nona-APD-HSA is a monosaccharide that belongs to the group of complex carbohydrates. It is a custom synthesis product, which has been synthesized by the methylation and glycosylation of a high purity oligosaccharide. The structural formula for this product is C14H30FNO6S2. This product is highly purified and has been fluorinated at one hydroxyl group. Sialyl-dimeric Lex-nona-APD-HSA has CAS No. 569078-29-4 and molecular weight of 432.5 g/mol.br>
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This product can be used as a synthetic sugar in various applications such as food, pharmaceuticals, cosmetics, and agrochemicals industries.br>
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The following are some properties of this compound:
1) Nonvolatile solids content: 98%

D-Xylose-BSA is an anaesthetic agent that is used to treat depression and postoperative pain. It is a natural compound that has been found in the blood cells of humans and animals. D-Xylose-BSA interacts with endogenous receptors for biotinylated D-xylose on granulocytes, which leads to activation of these cells and consequent release of inflammatory mediators. The ability of D-xylose-BSA to bind to microbial surfaces may be due to its chemical structure, which consists of a glycosilated hydrophilic part and a lipid part. D-Xylose-BSA also binds to polymorphonuclear leukocytes, postoperative erythrocytes, and replanted skin grafts.

1,4:3,6-Dianhydro-2,5-di-O-methyl-D-Iditol is a sugar modified with methyl groups and fluorine. It can be used as a building block for oligosaccharides and polysaccharides. The compound is synthesized from commercially available starting materials. 1,4:3,6-Dianhydro-2,5-di-O-methyl-D-Iditol is soluble in water and methanol. This product has not been studied for toxicity or carcinogenicity in animals.

2-Acetamido-1,3,6-tri-O-benzyl-2-deoxy-a-D-glucopyranoside is a carbohydrate that is composed of four sugar units. It is an antigenic determinant found on the surface of human erythrocytes. The chemical synthesis of this substance begins with the condensation reaction between D-glucose and 2,4,6,-trinitrophenylacetic acid followed by benzylation and acetylation. This compound belongs to the group of substances known as carbohydrates which are chains of monosaccharides that form glycosidic bonds with other sugars. These chains are classified according to their length and the number of sugar units they contain: trioses (three sugar units), tetroses (four sugar units), pentoses (five sugar units), hexoses (six sugar units) or heptoses (seven sugar).

The 4-Toluoyl-a-D-thiomannopyranoside is a six-membered ring with a hydrogen atom at the center. The structure of this molecule is composed of two chains, each of which has four atoms in their backbone. There are also two conformations to the molecule, one that can be observed as a chair conformation and one that can be seen as a boat conformation. In the chair conformation, there are three bonds that form from the central carbon atom to other carbons on the same chain. These bonds are called alpha bonds, and they connect in a linear fashion. In the boat conformation, these three bonds form an angle of 120 degrees with each other and have staggered geometry. The alpha bonds in this case form an angle of 180 degrees with each other.